HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → HCID 20432988, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Diethanolamine | HCID 8113 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 20432998 | HCID 20432998 | — |
| Product | HCID 20432988 | HCID 20432988 | — |
Reaction Steps
A mixture of 3-octadecylthiopropyl chloride (3.53 g., 0.01 mole), diethanolamine (2.1 g., 0.02 mole) and benzyl alcohol (5 ml.) is heated under reflux for one-half hour, then treated with an ethanolic solution of sodium hydroxide (0.4 g., 0.01 mole) and refluxed for five more minutes. The mixture is cooled, filtered, and the ethanol removed by evaporation. The benzyl alcohol is then removed by distillation in vacuo and the residue chromatographed on silica using first ether then methanol as eluants. The desired product is contained in the methanol eluate. It is isolated by evaporation of the solvent, m.p. 53°-54° C. Its hydrochloride salt melts at 65°-66° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04087552 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-ff23cbefc59344dc9beb2f061b6f9f4a |
| Source note | uspto-grants-1978_05 |